Directed evolution of angiotensin II-inhibiting peptides using a microbead display
2010
Gan, R., Nagoya Univ. (Japan) | Furuzawa, S. | Kojima, T. | Kanie, K. | Kato, R. | Okochi, M. | Honda, H. | Nakano, H.
Angiotensin II (ang II), an octapeptide (DRVYVHPF), can regulate blood pressure by binding specifically to its receptor, AT1. A peptide (VVIVIY) in the first transmembrane of AT1 has been found, via peptide array technology, to have an affinity for ang II. In this study, the peptide P2, which contained the VVIVIY sequence, was mutated and screened using microbead display' technology that utilized emulsion PCR and cell-free protein synthesis. After one round of screening, the binding activities of collected mutants were estimated using flow cytometry and a peptide array. Two of these exhibited improved association rate constants to ang II, compared to the P2 peptide.
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